Methods for selective leaching and extraction of precious metals in organic solvents

ABSTRACT

The present application relates to methods for leaching and extraction of precious metals. For example, the present application relates to methods of leaching gold, palladium and/or platinum from a substance comprising gold, palladium and/or platinum (such as a gold-containing ore or a platinum group metal (PGM) concentrate) using an organic solvent that is water-miscible or partially water-miscible.

FIELD

The present application relates to methods for leaching and extraction of precious metals. For example, the present application relates to methods of leaching gold, palladium and/or platinum from a substance comprising such precious metals (such as a gold-containing ore or a platinum group metal (PGM) concentrate) using an organic solvent that is water-miscible or partially water-miscible.

BACKGROUND

Gold is an element in the periodic table which belongs to the same group as silver and copper. It is usually found in combination with these metals in ores. The average concentration of copper and silver in Earth's crust is 50 and 0.07 ppm (parts per million) respectively while for gold it is just 0.005 ppm

Ore deposits with a concentration of 0.5 ppm or higher are considered to be economically recoverable. Due to its limited sources, gold recovery not only from ores, but also from secondary sources has become more and more important during the last decades. The annual production of go¹ld from the gold mining industry is more than 2500 tonnes worldwide². In addition, about 900 tonnes of secondary gold is recovered from different sources such as but not limited to anode slime and jewelry, dentistry and electronic scraps³.

The most commonly used process for gold recovery from ore includes the use of highly toxic inorganic cyanides (e.g., NaCN, KCN) to convert gold(0) into a water-soluble Au(CN)₂ ⁻ coordination complex by a process known as leaching. An example of a known process 10 for gold recovery using cyanide leaching is shown in FIG. 1. In process 10, low grade ore 12 is crushed and ground 14 then leached 16 with a basic solution of NaCN for 16 to 48 hours depending on ore type. Because of some environmental accidents in various gold mines around the world, gold leaching by cyanidation has been prohibited in many countries⁴. Therefore, considerable efforts have been made to find an alternative to cyanide and a variety of leaching reagents have been studied and proposed^(5,6).

Generally, following gold dissolution in the cyanide solution, gold is recovered by activated carbon adsorption (e.g. step 18 in process 10 of FIG. 1 wherein, for example 0.1 to 1 kg activated carbon per ton ore is used), or by the zinc cementation process. The activated carbon adsorption process is considerably more common^(7,8). For example, 4 to 8 kg gold can be adsorbed by 1 ton activated carbon in 4 to 8 steps over a time period of 4 to 8 hours.

As shown in FIG. 1, following the carbon adsorption step 18, the loaded activated carbon is washed 20 with low concentrated HCl to remove impurities such as adsorbed Zn, Ca, Fe, Cu and Ag then gold desorption (elution) 22 is done by using, for example 1% NaOH and 0.1 to 0.2% NaCN solution at a high temperature (e.g. 110° C.) for 36 to 72 hours. Pure gold 24 can be obtained, for example by electrowinning or reduction. The whole process time for gold recovery using a process like the process 10 shown in FIG. 1 is 46-110 hours.

Processes for gold recovery which use activated carbon may suffer from several drawbacks such as but not limited to low selectivity, very long procedures, loss of gold product, high temperature requirements, and further consumption of cyanide for desorption of gold from activated carbon, all of which may bring additional costs during the gold recovery process⁹.

Although considerable effort has been undertaken to replace cyanide, none of the reported leaching reagents has been used in the industrialization of gold production due, for example to drawbacks such as (i) high reagent consumption, (ii) complex chemistry, (iii) lack of industrial techniques for the recovery of gold from their resulting solutions, and (iv) low rate of gold recovery compared to cyanide. Drawbacks such as toxicity, cost, long reaction times and poor selectivity are also associated with known systems. Thus, it may be desirable to develop more effective leachants with, for example, higher efficiency and/or lower toxicity from both an environmental and an economical viewpoint.

Cyanide Leaching

For more than a century, cyanidation has remained the dominant process for extraction and recovery of gold from ore. Metallic gold can be dissolved in an alkaline solution of potassium or sodium cyanide in the presence of dissolved molecular oxygen (reaction 1):

In neutral or acidic conditions, over 99% of the cyanide will exist as highly poisonous HCN gas. By increasing pH, it is converted to free cyanide ion so that at a pH of 9.3, CN⁻ and HCN are in equilibrium, with 50% of each present. At a pH of 11, over 99% of the cyanide remains in solution as CN⁻.¹⁰ The free cyanide ion is a very strong ligand which can form a highly stable complex with gold, Au(CN)₂ ⁻, in aqueous solution. With stoichiometric ratios, gold dissolution in alkaline cyanide solution is slow, but by increasing the cyanide concentration, the leaching rate will increase until a maximum is reached (0.075 w/w % KCN or 0.06% NaCN) and after that the rate of dissolution remains constant¹¹.

Before cyanide treatment, the gold ore is typically crushed and ground to decrease the size of the ore particles to 75 microns or less to provide a larger contact surface area between the gold and the leaching solution. Depending on the ore type, the cyanide consumption varies from about 0.25 to 2 kg of cyanide per tonne of ore and the rate of gold dissolution in cyanide takes 16 to 48 hours¹¹. The cyanide consumption increases when the refractoriness of the gold ore is increased. A refractory gold ore is a gold-containing ore that is resistant to recovery by direct cyanidation. Other minerals and metals are also dissolved in the alkaline cyanide solution and they usually consume cyanide and oxygen and thus reduce the overall efficiency of gold leaching.

For example, copper minerals such as chalcocite (Cu₂S) and cuprite (Cu₂O) can form a variety of cyanide complexes such as CuCN, Cu(CN)₂ ⁻, Cu(CN)₃ ²⁻ and Cu(CN)₄ ³⁻ and iron sulfides like pyrrhotite (Fe₇S₈), pyrite (FeS₂) and arsenopyrite (FeAsS) form highly stable Fe(CN)₆ ⁴⁻ and Fe(CN)₆ ³⁻ complexes¹². In addition, most sulfide minerals have a detrimental effect on gold leaching since they may passivate the surface of gold and consume cyanide and oxygen. However, some other minerals such as galena (PbS) can improve gold leaching kinetics by preventing formation of a passivation layer on the gold surface¹³.

Although cyanide is still the main leaching reagent for gold recovery in the mining industry, it suffers from several drawbacks such as but not limited to high toxicity, slow leaching kinetics and low gold extraction for refractory ores. Considerable efforts have thus been made to find an alternative to cyanide.

Gold Recovery from Cyanide Solution

There are several techniques for gold recovery from cyanide leach liquors like carbon adsorption, zinc cementation and solvent extraction with carbon adsorption being by far the more common technique^(14,15). In the carbon adsorption technique, after gold is leached into cyanide solution, activated carbon is applied for selective gold adsorption to separate AuCN₂ ⁻ from other metals and impurities. 0.1 to 1 kg activated carbon per tonne of ore is usually applied in 4 to 8 steps for complete adsorption of Au(CN)₂ ⁻ complex from cyanide solution which takes 4 to 8 hours. The loaded activated carbon is usually washed with a low concentration HCl solution to remove other impurities such as Fe, Cu, Zn, Ca, and Ag. The dicyanoaurate(I) complex is then removed from the activated carbon in an elution step by washing the loaded activated carbon with a fresh basic sodium cyanide solution at 110° C. for 36 to 72 hours^(10,16). The desorbed Au(CN)₂ ⁻ complex is finally reduced to elemental gold by electrowinning or reduction.

The activated carbon method suffers from several drawbacks such as but not limited to low selectivity, very long procedures, loss of some gold product, and high temperature requirements¹⁷.

Alternatives to Cyanide

Due to the high toxicity and environmental problems of cyanide, there has been a quest to find useful alternatives. In recent years, some alternatives to cyanide have been reported to leach gold ore efficiently. Some of the useful reported leaching reagents are thiosulfate, thiocyanite, thiourea, and chloride in combination with an oxidizing agent like HNO₃, H₂O₂ and hypochlorite.

Thiosulfate Leaching

Thiosulfate is the most studied alternative to cyanide. Gold can be leached in alkaline aqueous solutions (pH=9.5-10.5) of thiosulfate in the presence of oxidizing agents like O₂ and copper(II) ions. The rate of gold dissolution becomes slower in the absence of copper (II) ions¹⁸. Ammonia is usually used to accelerate the rate of gold leaching in this media. It has an efficient role to stabilize the intermediate oxidation products of gold, decreasing the rate of thiosulfate oxidation by Cu²⁺, preventing the formation of insoluble components like sulfides on the gold surface and keeping a high concentration of Cu²⁺ by forming Cu(NH₃)₄ ²⁺ during the leaching process^(19,20). Oxygen has a dual role by oxidation of Cu(NH₃)₂ ⁺ to Cu(NH₃)₄ ²⁺ or direct oxidation of the gold surface. The overall balanced equation of gold dissolution in thiosulfate media is shown in the following reaction²¹ (2):

Compared to the cyanidation process, thiosulfate leaching has some advantages such as but not limited to fast leaching kinetics, lower toxicity and higher gold recovery in the case of some refractory gold ores^(22,23). However, it suffers from some major drawbacks such as but not limited to complex chemistry, toxicity of ammonia, ineffectiveness of activated carbon for desorption of leached gold, and high consumption of thiosulfate.

For example, the copper(II) itself consumes thiosulfate resulting in high consumption of both thiosulfate and copper and the resulting tetrathionate (S₄O₆ ²⁻) decomposes to elemental sulfur and forms sulfides such as CuS which increases the gold passivation during the leaching process (reaction 3)^(24,25).

Thiourea

Thiourea is another well-studied leaching reagent which can dissolve gold in acidic media based on the following reaction (4)²⁶:

Different oxidizing reagents such as but not limited to hydrogen peroxide, sodium peroxide, oxygen, ozone and ferric ion can be used in combination with thiourea to dissolve gold. Among these oxidizing reagents, ferric ion in sulfuric acid solution is a useful one (reaction 5)²⁷.

However, thiourea is not stable in acidic media in the presence of ferric ion and is decomposed to sulfur and cyanamide²⁸. Addition of a reducing agent such as SO₂ decreases the thiourea consumption by preventing its oxidation²⁹. The kinetics of gold leaching in thiourea solution are much faster than the cyanidation process because of nongaseous oxidants such as but not limited to hydrogen peroxide and ferric sulfate which are used instead of oxygen which is used in the cyanidation process³⁰. However, gold recovery and reagent consumption with cyanide is more economical than thiourea³¹.

Complexation with base metals such as copper accelerates thiourea consumption and decreases gold leaching kinetics. Thermal degradation, oxidation by the ferric sulfate and air are the other reasons for high consumption of thiourea³². Thiourea's commercial application has been hindered due to its high consumption and no existence of applicable industrial techniques for the recovery of gold from its solution. Although thiourea has a lower toxicity compared to cyanide, it is suspected to be a carcinogen agent and is treated with caution³³.

Chloride Solution Containing an Oxidizing Agent

Concentrated hydrochloric acid in combination with powerful oxidizing agents is known as a strong leaching reagent for leaching precious metals, for example from scraps and secondary sources³⁴. A hot solution of concentrated HCl mixed with concentrated HNO₃ (known as aqua regia) or hydrogen peroxide can dissolve gold according to the following chemical reactions (see reactions 6 and 7) resulting in the formation of a stable AuCl₄ ⁻ complex³⁵.

Apart from these oxidants, chlorine gas can also be used which forms the same gold species³⁶. Chlorine had been used to dissolve gold from ores and concentrates during the second half of the 19^(th) century until it was gradually replaced by the more economical alkaline cyanide leaching. In all cases, the dissolution rate is faster compared to cyanide, however, due to high concentration of HCl, all of these solutions are highly corrosive and toxic and in the case of gold ore treatment, their consumption is not economical³⁷.

Chloride/Hypochlorite

Chloride/hypochlorite solutions have been recognized as another alternative leaching reagent to cyanide which can dissolve gold in a wide range of pH values³⁸. Depending on the solution's pH, three different oxidizing species can be formed in hypochlorite solutions. At pH>7.5, hypochlorite ion (OCl⁻) is the dominant species while for pH values between 3.5 and 7.5, hypochlorous acid (HOCl) acts as oxidizing agent and for pH less than 3.5, nascent chlorine gas (Cl₂) is formed. Among these three species, HOCl is the most effective oxidizing agent to leach gold as the [AuCl₄]⁻ (reaction 8)³⁹.

In a solution containing 100 g/L NaCl, the [AuCl₄]⁻ is stable in the pH range of 0-8 and potentials greater than 0.9 V⁴⁰. The chloride-hypochlorite solution is a useful leaching reagent, for example for refractory gold ores. Because of low acidity, it does not produce a corrosion media; however the reagents consumption is still high^(41,42). The main drawback of this leaching reagent is that the percentage of leached gold is usually less than 85%⁴³.

Gold Leaching in Organic Solvents

Polar and water miscible organic solvents have been investigated for dissolution of some transition metals like silver and copper^(44,45,46.) In some cases better leaching efficiency has been achieved in particular mixtures of water-solvent or pure solvent. There are also a few examples of gold leaching in organic solvents like DMSO, methanol, acetone, N,N-dimethylformamide and acetonitrile^(45,47,48). For example, Yukimichi investigated the dissolution rate of gold, silver and palladium in different halogen-halide-polar organic solvent systems and in the case of gold, he proved it could be dissolved in a mixture of a halide source, a halogen such as chlorine gas, bromine, iodine, and an organic solvent like methanol or MeCN. Among investigated systems, mixtures of chlorine gas, acetonitrile and Me₃NHCl (as chloride source) dissolved gold most effectively; even faster than aqua regia⁴⁸.

SUMMARY

The present studies disclose the use of a polar, water-miscible or partially water-miscible organic solvent in combination with conventional leaching reagents. Conventional leaching reagents, for example, acidified chloride solutions containing an oxidizing agent have not been investigated for gold leaching directly in organic solvents. This new recovery system may, for example, simplify the recovery process, save considerable time and energy and due to the recoverability of the organic solvent, produce less waste.

Accordingly, the present application includes a method of leaching gold, palladium and/or platinum from a substance comprising gold, palladium and/or platinum, the method comprising contacting the substance with a mixture comprising:

(a) an acid;

(b) an oxidizing agent; and

(c) a water-miscible or partially water-miscible organic solvent,

under conditions to leach the gold, palladium and/or platinum from the substance.

In another embodiment of the present application, the conditions to leach the gold, palladium and/or platinum from the substance comprise stirring the substance and the mixture for a time of about 0.1 minute to about 30 minutes at a temperature of about 10° C. to about 80° C.

In an embodiment, the acid in the mixture is selected from HCl, H₂SO₄, HBr, HNO₃, H₃PO₄ and HI.

In another embodiment, the acid is an aqueous solution of HCl having a concentration of from about 0.01 M to about 2.5 M.

In an embodiment, the oxidizing agent in the mixture is selected from H₂O₂, Cl₂, Br₂, I₂, Ca(ClO)₂, HNO₃, MnO₂, KMnO₄ and K₂Cr₂O₇. In another embodiment, the oxidizing agent is H₂O₂ or Ca(ClO)₂.

In another embodiment of the present application, the water-miscible or partially water-miscible organic solvent in the mixture is selected from acetic acid, ethyl acetate and acetonitrile.

In an embodiment, the mixture further comprises a metal halide, an ammonium halide, a tetraalkylammonium halide or a combination thereof. In another embodiment, the mixture further comprises the metal halide and the metal halide is CaCl₂. In a further embodiment, the CaCl₂ in the mixture has a concentration of from about 0.05M to about 1.5M. It is an embodiment of the present application that reagent (a) in the mixture is HCl, reagent (b) in the mixture is H₂O₂ and reagent (c) in the mixture is acetic acid.

In an embodiment, the substance comprising gold, palladium and/or platinum is a gold-containing substance. In an embodiment, the gold-containing substance further comprises iron, copper, cobalt, or nickel or a combination thereof, and the method selectively dissolves the gold from the gold-containing substance. In another embodiment of the present application, the gold-containing substance is a gold-containing ore.

In an embodiment, the method provides a gold dissolution rate of at least 500 gm⁻² h⁻¹, at least 1000 gm⁻² h⁻¹ or at least 5000 gm⁻² h⁻¹. In another embodiment, the method provides a gold dissolution rate of about 500 gm⁻² h⁻¹ to about 9500 gm⁻² h⁻¹ or about 1000 gm⁻² h⁻¹ to about 9500 gm⁻² h⁻¹.

In an alternative embodiment, the substance comprising gold, palladium and/or platinum is a platinum group metal concentrate.

In an embodiment, the method further comprises:

-   -   separating the water-miscible or partially water-miscible         organic solvent containing the leached gold, palladium and/or         platinum from insoluble impurities; and     -   evaporating the water-miscible or partially water-miscible         organic solvent from the leached gold, palladium and/or         platinum.

In another embodiment, the method further comprises, after evaporating, treating the leached gold, palladium and/or platinum with a compound of Formula I:

wherein

R¹ is —NR⁴R⁵ or aryl;

R² and R³ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

R⁴ and R⁵ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R⁴ and R⁵ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

X is O or S;

Y is S, NR⁶ or CR⁶R⁷; and

R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl,

under conditions to form a complex between the compound of Formula I and the leached gold and/or palladium.

In an embodiment, the compound of Formula I is a compound of Formula I(a):

wherein R², R³, R⁴, R⁵ and Y are as defined for the compound of Formula I.

In an embodiment, the conditions to form the complex between the compound of Formula I and the leached gold and/or palladium comprise treating the leached gold, palladium and/or platinum with the compound of Formula I in a water-immiscible organic solvent for a time of about 2 minutes to about 30 minutes at a temperature of about 10° C. to about 40° C.

In another embodiment, the water-immiscible organic solvent is dichloromethane, chloroform, chlorobenzene or toluene.

In an embodiment, the method further comprises stripping the gold and/or palladium from the complex between the compound of Formula I and the leached gold and/or palladium by a method comprising treating the water-immiscible organic solvent containing the complex between the compound of Formula I and the leached gold and/or palladium with an aqueous solution comprising an acid and thiourea under conditions to obtain a gold and/or palladium-containing strip solution and a gold and/or palladium-reduced organic phase comprising the compound of Formula I.

In another embodiment, the method further comprises separating the gold and/or palladium-containing strip solution from the gold and/or palladium-reduced organic phase comprising the compound of Formula I and recovering gold and/or palladium from the gold and/or palladium-containing strip solution by electrowinning or reduction.

In an alternative embodiment, the method further comprises:

-   -   separating the water-miscible or partially water-miscible         organic solvent containing the leached gold, palladium and/or         platinum from insoluble impurities;     -   treating the leached gold, palladium and/or platinum in the         water-miscible or partially water-miscible organic solvent with         a reducing agent under conditions to obtain gold, palladium         and/or platinum; and     -   separating the gold, palladium and/or platinum from the         water-miscible or partially water-miscible organic solvent.

In an embodiment, the reducing agent is selected from NaBH₄, ferrocene, Fe powder and Zn powder.

In another embodiment, the method further comprises recycling the water-miscible or partially water-miscible organic solvent.

In an embodiment, the method further comprises, after separating the gold, palladium and/or platinum from the water-miscible or partially water-miscible organic solvent:

dissolving the gold, palladium and/or platinum in aqua regia; and

treating the dissolved gold, palladium and/or platinum with a compound of Formula I:

wherein

R¹ is —NR⁴R⁵ or aryl;

R² and R³ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

R⁴ and R⁵ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R⁴ and R⁵ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

X is O or S;

Y is S, NR⁶ or CR⁶R⁷; and

R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl,

under conditions to form a complex between the compound of Formula I and the dissolved gold and/or palladium.

In an embodiment, the conditions to form the complex between the compound of Formula I and the dissolved gold and/or palladium comprise treating the dissolved gold, palladium and/or platinum with the compound of Formula I in a water-immiscible organic solvent for a time of about 2 minutes to about 30 minutes at a temperature of about 10° C. to about 40° C.

In another embodiment, the water-immiscible organic solvent is dichloromethane, chloroform, chlorobenzene or toluene.

In an embodiment, the method further comprises stripping the gold and/or palladium from the complex between the compound of Formula I and the dissolved gold and/or palladium by a method comprising contacting the water-immiscible organic solvent containing the complex between the compound of Formula I and the dissolved gold and/or palladium with an aqueous solution comprising an acid and thiourea under conditions to obtain a gold and/or palladium-containing strip solution and a gold and/or palladium-reduced organic phase comprising the compound of Formula I.

In another embodiment, the method further comprises separating the gold and/or palladium-containing strip solution from the gold and/or palladium-reduced organic phase comprising the compound of Formula I and recovering gold and/or palladium from the gold and/or palladium-containing strip solution by electrowinning or reduction.

Other features and advantages of the present application will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples, while indicating embodiments of the application, are given by way of illustration only and the scope of the claims should not be limited by these embodiments, but should be given the broadest interpretation consistent with the description as a whole.

BRIEF DESCRIPTION OF THE DRAWINGS

The present application will now be described in greater detail with reference to the drawings in which:

FIG. 1 shows a schematic representation of a process of gold recovery using cyanide leaching according to the prior art.

FIG. 2 is a plot showing Au Recovery (%) as a function of time (hours) for simultaneous leaching and extraction according to an embodiment of a method of the present application in comparison to conventional leaching.

FIG. 3 shows a schematic representation of a method of leaching and extracting gold from a gold-containing substance.

FIG. 4 shows a schematic representation of a method of leaching gold from a gold-containing substance according to an embodiment of a method of the present application.

FIG. 5 is a plot showing comparison studies of gold dissolution rate between aqua regia, concentrated HCl/H₂O₂, and acetic acid systems.

FIG. 6 shows competitive studies of dissolution rates of gold vs. base metals in: (a) Concentrated HCl/H₂O₂ mixture (four parts HCl (37%) and one part H₂O₂ (30%)) vs. acetic acid (including 1.5 M HCl, 0.6 M H₂O₂, and 0.6 M CaCl₂) (b) Acetonitrile solution (including 1 M HCl and 0.2 M H₂O₂) vs. acetic acid (including 0.5 M HCl, 0.2 M H₂O₂, and 0.2 M CaCl₂).

DETAILED DESCRIPTION

I. Definitions

Unless otherwise indicated, the definitions and embodiments described in this and other sections are intended to be applicable to all embodiments and aspects of the present application herein described for which they are suitable as would be understood by a person skilled in the art.

The term “compound of the present application” and the like as used herein refers to a compound of Formula I as defined herein.

In understanding the scope of the present application, the term “comprising” and its derivatives, as used herein, are intended to be open ended terms that specify the presence of the stated features, elements, components, groups, integers, and/or steps, but do not exclude the presence of other unstated features, elements, components, groups, integers and/or steps. The foregoing also applies to words having similar meanings such as the terms, “including”, “having” and their derivatives. The term “consisting” and its derivatives, as used herein, are intended to be closed terms that specify the presence of the stated features, elements, components, groups, integers, and/or steps, but exclude the presence of other unstated features, elements, components, groups, integers and/or steps. The term “consisting essentially of”, as used herein, is intended to specify the presence of the stated features, elements, components, groups, integers, and/or steps as well as those that do not materially affect the basic and novel characteristic(s) of features, elements, components, groups, integers, and/or steps.

Terms of degree such as “substantially”, “about” and “approximately” as used herein mean a reasonable amount of deviation of the modified term such that the end result is not significantly changed. These terms of degree should be construed as including a deviation of at least ±5% of the modified term if this deviation would not negate the meaning of the word it modifies.

The term “and/or” as used herein means that the listed items are present, or used, individually or in combination. In effect, this term means that “at least one of” or “one or more” of the listed items is used or present.

As used in this application, the singular forms “a”, “an” and “the” include plural references unless the content clearly dictates otherwise. For example, an embodiment including “a compound” should be understood to present certain aspects with one compound or two or more additional compounds.

In embodiments comprising an “additional” or “second” component, such as an additional or second compound, the second component as used herein is chemically different from the other components or first component. A “third” component is different from the other, first, and second components, and further enumerated or “additional” components are similarly different.

In embodiments of the present application, the compounds described herein have at least one asymmetric center. Where compounds possess more than one asymmetric center, they may exist as diastereomers. It is to be understood that all such isomers and mixtures thereof in any proportion are encompassed within the scope of the present application. It is to be further understood that while the stereochemistry of the compounds may be as shown in any given compound listed herein, such compounds may also contain certain amounts (for example, less than 20%, suitably less than 10%, more suitably less than 5%) of compounds of the present application having alternate stereochemistry. It is intended that any optical isomers, as separated, pure or partially purified optical isomers or racemic mixtures thereof are included within the scope of the present application.

The term “suitable” as used herein means that the selection of specific reagents or conditions will depend on the reaction being performed and the desired results, but none-the-less, can generally be made by a person skilled in the art once all relevant information is known.

The term “immiscible” as used herein when referring to two liquid phases means that the two liquid phases cannot be mixed to form a solution having a single phase under the conditions used, such as the relative proportions of the two liquid phases and/or the temperature, etc. Two immiscible liquid phases will, for example separate into two liquid phases after mixing. Each of these two liquid phases may, for example contain small amounts of the other liquid phase. Accordingly, a “water-immiscible” liquid such as a “water-immiscible organic solvent” is a liquid that cannot be mixed with water to form a solution having a single phase under the conditions used but that may, for example contain small amounts of water after being mixed with water.

The term “partially miscible” as used herein when referring to two liquid phases means that the two liquid phases will, for example, separate into two liquid phases after mixing, each liquid phase containing a portion of the other liquid phase in a dissolved state. Accordingly, a “partially water-miscible organic solvent” is a liquid that, after mixing with water, will separate into two liquid phases after mixing, one phase being water containing a portion, for example, about 10% (v/v) of the partially water-miscible organic liquid in a dissolved state, and the other phase being the partially water-miscible organic liquid containing a portion, for example, about 10% (v/v) of water in a dissolved state.

The term “miscible” as used herein when referring to two liquid phases means that the two liquid phases can, for example be mixed in all proportions to form a homogeneous solution. Two miscible liquid phases will not, for example separate into two liquid phases after mixing. Accordingly, a “water-miscible” liquid such as a “water-miscible organic solvent” is a liquid that can be mixed with water to form a homogeneous solution.

The term “alkyl” as used herein, whether it is used alone or as part of another group, means straight or branched chain, saturated alkyl groups. The number of carbon atoms that are possible in the referenced alkyl group are indicated by the numerical prefix “C_(n1-n2)”. For example, the term C₁₋₁₀alkyl means an alkyl group having 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms.

The term “alkylene” as used herein, whether it is used alone or as part of another group, means straight or branched chain, saturated alkylene group, that is, a saturated carbon chain that contains substituents on two of its ends. The number of carbon atoms that are possible in the referenced alkylene group are indicated by the numerical prefix “C_(n1-n2)”. For example, the term C₁₋₆alkylene means an alkylene group having 1, 2, 3, 4, 5 or 6 carbon atoms.

The term “cycloalkyl,” as used herein, whether it is used alone or as part of another group, means saturated alkyl groups having at least one cyclic ring. The number of carbon atoms that are possible in the referenced cycloalkyl group are indicated by the numerical prefix “C_(n1-n2)”. For example, the term C₃₋₁₀cycloalkyl means a cycloalkyl group having 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms.

The term “heterocycloalkyl” as used herein, whether it is used alone or as part of another group, refers to a non-aromatic, ring-containing group having one or more multivalent heteroatoms, independently selected from N, O and S, as a part of the ring structure and including at least 3 and up to 20 atoms in the ring(s). Heterocycloalkyl groups are either saturated or unsaturated (i.e. contain one or more double bonds) and may contain more than one ring.

The term “aryl” as used herein, whether it is used alone or as part of another group, refers to cyclic groups that contain at least one aromatic ring. In an embodiment of the application, the aryl group contains from 6, 9, 10 or 14 atoms, such as phenyl, naphthyl, indanyl or anthracenyl.

The term “heteroaryl” as used herein, whether it is used alone or as part of another group, refers to an aromatic, ring-containing group having one or more multivalent heteroatoms, independently selected from N, O and S, as a part of the ring structure and including at least 5 and up to 20 atoms in the ring(s). Heteroaryl groups may contain more than one ring.

II. Methods of the Application

The present studies disclose the use of a polar, water-miscible or partially water-miscible organic solvent in combination with conventional leaching reagents. Conventional leaching reagents, for example, acidified chloride solutions containing an oxidizing agent have not been investigated for gold leaching directly in organic solvents. A number of leaching reagents were investigated in the present studies. Using mixtures of HCl with H₂O₂ or Ca(ClO)₂ in ethyl acetate or acetonitrile achieved greater than 99.9% gold leaching in a short period of time with 1M HCl using a very low concentration of the oxidant. The results show that these new leaching systems can dissolve gold much more rapidly than even aqua regia despite the relevant concentrations of leaching materials being much lower. The leached gold can then be precipitated out from the ethyl acetate or acetonitrile solution, for example, by direct reduction of AuCl₄ ⁻ by NaBH₄, zinc or ferrocene. Because some other impurities can be reduced during gold reduction, the resulting gold precipitate can then be purified by solvent extraction using, for example a compound of Formula I as defined herein. In some embodiments, this new recovery system, for example, simplifies the recovery process, saves considerable time and energy and due, to the recoverability of the organic solvent, produces less waste.

Accordingly, the present application includes a method of leaching gold, palladium and/or platinum from a substance comprising gold, palladium and/or platinum, the method comprising contacting the substance with a mixture comprising:

(a) an acid;

(b) an oxidizing agent; and

(c) a water-miscible or partially water-miscible organic solvent,

under conditions to leach the gold, palladium and/or platinum from the substance.

In an embodiment, the method further comprises:

-   -   separating the water-miscible or partially water-miscible         organic solvent containing the leached gold, palladium and/or         platinum from insoluble impurities; and     -   evaporating the water-miscible or partially water-miscible         organic solvent from the leached gold, palladium and/or         platinum.

The water-miscible or partially water-miscible organic solvent containing the leached gold, palladium and/or platinum and the insoluble impurities are separated by any suitable means, the selection of which can be made by a person skilled in the art.

The water-miscible or partially water-miscible organic solvent is evaporated from the leached gold, palladium and/or platinum by any suitable means, the selection of which can be made by a person skilled in the art. In an embodiment, distillation is used for evaporating the water-miscible or partially water-miscible organic solvent from the leached gold, palladium and/or platinum.

In another embodiment, the method further comprises, after evaporating, treating the leached gold, palladium and/or platinum with a compound of Formula I:

wherein

R¹ is —NR⁴R⁵ or aryl;

R² and R³ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

R⁴ and R⁵ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R⁴ and R⁵ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

X is O or S;

Y is S, NR⁶ or CR⁶R⁷; and

R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl,

under conditions to form a complex between the compound of Formula I and the leached gold and/or palladium. Under such conditions, platinum does not, for example, form a complex with the compound of Formula I.

In an embodiment, R¹ is —NR⁴R⁵.

In an alternative embodiment, R¹ is aryl. In another embodiment, R¹ is C₆₋₁₀aryl. In a further embodiment, R¹ is phenyl.

In another embodiment, the compound of Formula I is a compound of Formula I(a):

wherein R², R³, R⁴, R⁵ and Y are as defined for the compound of Formula I.

In an embodiment of the present application, for example, in the compound of Formula I(a), only one of R², R³, R⁴ and R⁵ is H.

In another embodiment of the present application, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl, a heteroaryl or a substituted heterocycloalkyl or a substituted heteroaryl.

In an embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form a heterocycloalkyl or a substituted heterocycloalkyl. In another embodiment, example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form a heterocycloalkyl or a substituted heterocycloalkyl, wherein heterocycloalkyl is selected from aziridinyl, azetidinyl, pyrrolidinyl, piperidinyl, azepanyl, azocanyl, imidazolidinyl, oxazolidinyl, thiazolidinyl, piperazinyl, hexahydropyrimidinyl, morpholinyl, 1,3-oxazinanyl, thiomorpholinyl, 1,3-thiazinanyl, 1,3-diazepanyl, 1,3-oxazepanyl, 1,3-thiazepanyl, 1,4-diazepanyl, 1,4-oxazepanyl, 1,4-thiazepanyl, 1,3-diazocanyl, 1,3-oxazocanyl, 1,3-thiazocanyl, 1,4-diazocanyl, 1,4-oxazocanyl, 1,4-thiazocanyl, 1,5-diazocanyl, 1,5-oxazocanyl and 1,5-thiazocanyl. In a further embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form morpholinyl, pyrrolidinyl or 4-methylpiperidinyl. In an embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form morpholinyl. In another embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form pyrrolidinyl. In a further embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form 4-methylpiperidinyl.

In an embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form a heteroaryl or a substituted heteroaryl. In another embodiment of the present application, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form a heteroaryl. In a further embodiment, for example, in the compound of Formula I(a), R² and R³ together with the nitrogen atom to which they are attached form a heteroaryl selected from pyrrolyl, imidazolyl, pyrazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, furazanyl, pyridinyl, pyrazinyl, pyrimidinyl, pyridazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl and 1,3,5-triazinyl.

In an embodiment, for example, in the compound of Formula I(a), R⁴ is selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl. In another embodiment, for example, in the compound of Formula I(a), R⁴ is selected from H, C₁₋₆alkyl, C₃₋₈cycloalkyl, C₁₋₄alkyleneC₃₋₈cycloalkyl, heterocycloalkyl and phenyl. In a further embodiment, for example, in the compound of Formula I(a), R⁴ is selected from H, C₁₋₆alkyl and C₃₋₈cycloalkyl. It is an embodiment that, for example, in the compound of Formula I(a), R⁴ is selected from H and C₁₋₄alkyl. In another embodiment of the present application, for example, in the compound of Formula I(a), R⁴ is H.

In an embodiment, for example, in the compound of Formula I(a), R⁵ is selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl. In another embodiment, for example, in the compound of Formula I(a), R⁵ is selected from C₃₋₁₀alkyl, C₃₋₈cycloalkyl, C₁₋₄alkyleneC₃₋₈cycloalkyl, heterocycloalkyl and phenyl. In a further embodiment, for example, in the compound of Formula I(a), R⁵ is selected from C₁₋₆alkyl and C₃₋₈cycloalkyl. It is an embodiment, for example, in the compound of Formula I(a), that R⁵ is isopropyl or cyclohexyl. In another embodiment, for example, in the compound of Formula I(a), R⁵ is isopropyl. In a further embodiment, for example, in the compound of Formula I(a), R⁵ is cyclohexyl.

In an embodiment, at least one of any one of R¹ to R⁷ is aryl. In another embodiment, at least one of any one of R¹ to R⁷ is phenyl.

In an embodiment, for example, in the compound of Formula I(a), R⁴ is H or C₁₋₄alkyl and R⁵ is C₁₋₆alkyl or C₃₋₈cycloalkyl. In another embodiment, for example, in the compound of Formula I(a), R⁴ is H and R⁵ is C₁₋₆alkyl or C₃₋₈cycloalkyl. In a further embodiment of the present application, for example, in the compound of Formula I(a), R⁴ is H and R⁵ is C₁₋₆alkyl. It is an embodiment, for example, in the compound of Formula I(a), that R⁴ is H and R⁵ is C₃₋₈cycloalkyl. In another embodiment, for example, in the compound of Formula I(a), R⁴ is H and R⁵ is isopropyl. In a further embodiment, for example, in the compound of Formula I(a), R⁴ is H and R⁵ is cyclohexyl.

In an embodiment, X is O. In another embodiment, X is S.

In an embodiment, Y is NR⁶.

In an embodiment, R⁶ is selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl. In another embodiment, R⁶ is selected from H, C₁₋₆alkyl, C₃₋₈cycloalkyl, C₁₋₄alkyleneC₃₋₈cycloalkyl and heterocycloalkyl. In a further embodiment, R⁶ is H, C₁₋₆alkyl or C₃₋₈cycloalkyl. It is an embodiment that R⁶ is H. In another embodiment R⁶ is C₁₋₆alkyl. In another embodiment of the present application, R⁶ is C₃₋₈cycloalkyl. In a further embodiment, R⁶ is isopropyl. It is an embodiment that R⁶ is cyclohexyl.

In an embodiment, Y is CR⁶R⁷.

In an embodiment, R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl. In another embodiment, R⁶ and R⁷ are each independently selected from H, C₁₋₆alkyl, C₃₋₈cycloalkyl, C₁₋₄alkyleneC₃₋₈cycloalkyl and heterocycloalkyl. In a further embodiment, R⁶ and R⁷ are each independently H, C₁₋₆alkyl or C₃₋₈cycloalkyl.

In an embodiment, the compound of Formula I is a compound of Formula I(a)(i), I(a)(ii), I(a)(iii) or I(a)(iv):

In another embodiment of the present application, the compound of Formula I is the compound of Formula I(a)(i):

In another embodiment of the present application, the compound of Formula I is the compound of Formula I(a)(ii):

In another embodiment of the present application, the compound of Formula I is the compound of Formula I(a)(iii):

In another embodiment of the present application, the compound of Formula I is the compound of Formula I(a)(iv):

In another embodiment, the compound of Formula I is a compound of Formula I(b)(i):

In another embodiment, the compound of Formula I is a compound of Formula I(c)(i), I(c)(ii), I(c)(iii) or I(c)(iv):

wherein in each of the compounds of Formula I(c)(i), I(c)(ii), I(c)(iii) or I(c)(iv) independently, one of Z¹ and Z² is O and the other of Z¹ and Z² is S.

In an embodiment, the compounds of Formula I are commercially available or are prepared using methods known in the literature from commercially available materials. For example, a compound of Formula I(a) is prepared by adding an appropriately substituted amine to a mixture of CS₂ and a carbodiimide in a suitable polar solvent, such as an alcoholic solvent, under conditions to form the compound of Formula I(a). The compound of Formula I(a) will generally precipitate from the reaction mixture and is isolated and, optionally, purified using known methods. In an embodiment, a slight excess, for example 1.05 to 1.5, suitably 1.1, equivalents of the amine and CS₂ are used. In an embodiment, the suitable solvent is methanol or ethanol, suitably methanol. In an embodiment the reaction is performed at or around room temperature, however the temperature can be adjusted as needed by a person skilled in the art.

In an embodiment, the conditions to form the complex between the compound of Formula I and the leached gold and/or palladium comprise treating the leached gold, palladium and/or platinum with the compound of Formula I in a water-immiscible organic solvent for a time of about 2 minutes to about 30 minutes at a temperature of about 10° C. to about 40° C. It will be appreciated by a person skilled in the art that platinum remains in the aqueous phase and is not extracted to the organic phase by the compound of Formula I. Platinum can be recovered from the aqueous phase by any suitable method, the selection of which can be made by a person skilled in the art.

In an embodiment, the molar ratio of the compound of Formula I to the gold and/or palladium is about 1:10 to about 50:1. In another embodiment, the molar ratio of the compound of Formula I to the gold and/or palladium is about 1:1 to about 20:1. In a further embodiment, the molar ratio of the compound of Formula I to the gold and/or palladium is about 2:1 to about 10:1. It is an embodiment that the molar ratio of the compound of Formula Ito the gold and/or palladium is about 3:1 to about 4:1. In another embodiment, the molar ratio of the compound of Formula I to the gold and/or palladium is about 3:1. In a further embodiment, the molar ratio of the compound of Formula I to the gold and/or palladium is about 4:1.

In an embodiment, the water-immiscible organic solvent is dichloromethane, chloroform, chlorobenzene or toluene. In another embodiment, the water-immiscible organic solvent is dichloromethane.

In another embodiment, the method further comprises stripping the gold and/or palladium from the complex between the compound of Formula I and the leached gold and/or palladium by a method comprising treating the water-immiscible organic solvent containing the complex between the compound of Formula I and the leached gold and/or palladium with an aqueous solution comprising an acid and thiourea under conditions to obtain a gold and/or palladium-containing strip solution and a gold and/or palladium-reduced organic phase comprising the compound of Formula I. In an embodiment, the conditions to obtain a gold and/or palladium-containing strip solution and a gold and/or palladium-reduced organic phase comprise stirring the water-immiscible organic solvent with an aqueous solution comprising H₂SO₄, for example 1M H₂SO₄ and thiourea, for example 0.7 M thiourea for a time of about 5 minutes to about 1 hour or about 15 minutes at a temperature of about 10° C. to about 40° C. or about 20° C. to about 25° C. Other suitable acids such as but not limited to HCl may be used in the stripping step. However, it will be appreciated by a person skilled in the art that HCl is corrosive and that HCl gas may come out from the solution during subsequent reduction or electrowinning.

In a further embodiment, the method further comprises separating the gold and/or palladium-containing strip solution from the gold and/or palladium-reduced organic phase comprising the compound of Formula I and recovering gold and/or palladium from the gold and/or palladium-containing strip solution by electrowinning or reduction. The gold and/or palladium-containing strip solution and the gold and/or palladium-reduced organic phase comprising the compound of Formula I are separated by any suitable means, the selection of which for use in the methods of the present application can be made by a person skilled in the art.

In an alternative embodiment, the method further comprises:

-   -   separating the water-miscible or partially water-miscible         organic solvent containing the leached gold, palladium and/or         platinum from insoluble impurities;     -   treating the leached gold, palladium and/or platinum in the         water-miscible or partially water-miscible organic solvent with         a reducing agent under conditions to obtain gold, palladium         and/or platinum; and     -   separating the gold, palladium and/or platinum from the         water-miscible or partially water-miscible organic solvent.

The water-miscible or partially water-miscible organic solvent containing the leached gold, palladium and/or platinum and the insoluble impurities are separated by any suitable means, the selection of which can be made by a person skilled in the art. The gold, palladium and/or platinum and the water-miscible or partially water-miscible organic solvent are separated by any suitable means, the selection of which can be made by a person skilled in the art.

The reducing agent can be any suitable reducing agent. In an embodiment of the present application, the reducing agent is selected from NaBH₄, ferrocene, Fe powder and Zn powder.

In another embodiment, the method further comprises recycling the water-miscible or partially water-miscible organic solvent.

In an embodiment, the method further comprises, after separating the gold, palladium and/or platinum from the water-miscible or partially water-miscible organic solvent:

dissolving the gold, palladium and/or platinum in aqua regia; and

treating the dissolved gold, palladium and/or platinum with a compound of Formula I:

wherein

R¹ is —NR⁴R⁵ or aryl;

R² and R³ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

R⁴ and R⁵ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or

R⁴ and R⁵ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl;

X is O or S;

Y is S, NR⁶ or CR⁶R⁷; and

R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl,

under conditions to form a complex between the compound of Formula I and the dissolved gold and/or palladium. Under such conditions, platinum does not, for example, form a complex with the compound of Formula I. The compound of Formula I can be varied as detailed herein.

In another embodiment, the conditions to form the complex between the compound of Formula I and the dissolved gold and/or palladium comprise treating the dissolved gold, palladium and/or platinum with the compound of Formula I in a water-immiscible organic solvent for a time of about 2 minutes to about 30 minutes at a temperature of about 10° C. to about 40° C. It will be appreciated by a person skilled in the art that platinum remains in the aqueous phase and is not extracted to the organic phase by the compound of Formula I. Platinum can be recovered from the aqueous phase by any suitable method, the selection of which can be made by a person skilled in the art.

In an embodiment, the water-immiscible organic solvent is dichloromethane, chloroform, chlorobenzene or toluene. In another embodiment, the water-immiscible organic solvent is dichloromethane.

In an embodiment, the method further comprises stripping the gold and/or palladium from the complex between the compound of Formula I and the dissolved gold and/or palladium by a method comprising contacting the water-immiscible organic solvent containing the complex between the compound of Formula I and the dissolved gold and/or palladium with an aqueous solution comprising an acid and thiourea under conditions to obtain a gold and/or palladium-containing strip solution and a gold and/or palladium-reduced organic phase comprising the compound of Formula I. In an embodiment, the conditions to obtain a gold and/or palladium-containing strip solution and a gold and/or palladium-reduced organic phase comprise stirring the water-immiscible organic solvent with an aqueous solution comprising H₂SO₄, for example 1M H₂SO₄ and thiourea, for example 0.7 M thiourea for a time of about 5 minutes to about 1 hour or about 15 minutes at a temperature of about 10° C. to about 40° C. or about 20° C. to about 25° C. Other suitable acids such as but not limited to HCl may be used in the stripping step. However, it will be appreciated by a person skilled in the art that HCl is corrosive and that HCl gas may come out from the solution during subsequent reduction or electrowinning.

In another embodiment, the method further comprises separating the gold and/or palladium-containing strip solution from the gold and/or palladium-reduced organic phase comprising the compound of Formula I and recovering gold and/or palladium from the gold and/or palladium-containing strip solution by electrowinning or reduction. The gold and/or palladium-containing strip solution and the gold and/or palladium-reduced organic phase comprising the compound of Formula I are separated by any suitable means, the selection of which for use in the methods of the present application can be made by a person skilled in the art.

In an embodiment, the gold and/or palladium is recovered from the gold and/or palladium-containing strip solution by electrowinning.

In another embodiment, the gold and/or palladium is recovered from the gold and/or palladium-containing strip solution by reduction. The reducing agent can be any suitable reducing agent. In an embodiment, the reducing agent is oxalic acid, Zn powder, Fe powder or NaBH₄. In an embodiment, the reducing agent is NaBH₄ and a temperature of from about 10° C. to about 35° C. or about 20° C. to about 25° C. is used. In another embodiment, the reducing agent is oxalic acid and a temperature of from about 40° C. to about 60° C. or about 50° C. is used.

In an embodiment, the conditions to leach the gold, palladium and/or platinum from the gold, palladium and/or platinum-containing substance comprise stirring the gold, palladium and/or platinum-containing substance and the mixture for a time of about 0.1 minute to about 4 hours, about 0.1 minute to about 2 hours, about 0.1 minute to about 30 minutes or less than about 15 minutes at a temperature of about 10° C. to about 80° C., about 10° C. to about 40° C. or about 20° C. to about 25° C.

The acid in the mixture can be any suitable acid; i.e. the acid in the mixture can be any suitable proton donor. In an embodiment, the acid is a hydrogen halide (e.g., HCl, HBr or HI), chlorous acid, chloric acid, bromous acid, bromic acid, iodous acid, iodic acid, perchloric acid, sulfuric acid, nitric acid, oxalic acid, phosphoric acid, an organic acid (e.g., benzenesulfonic acid) or combinations thereof. In an embodiment, the acid is selected from HCl, H₂SO₄, HBr, HNO₃, H₃PO₄ and HI. In another embodiment, the acid is selected from HCl, H₂SO₄, HBr and HI. In another embodiment, the acid is HCl. The concentration of the acid can be any suitable concentration. In an embodiment, the acid is an aqueous solution of HCl having a concentration of from about 0.01 M to about 4 M. In a further embodiment, the acid is an aqueous solution of HCl having a concentration of from about 0.5 M to about 4 M. It is an embodiment that the acid is an aqueous solution of HCl having a concentration of from about 1 M to about 2.5 M, about 0.1 M to about 2.5 M or about 0.01 M to about 2.5 M. In another embodiment, the acid is an aqueous solution of HCl having a concentration of about 2 M. In a further embodiment of the present application, the acid is an aqueous solution of HCl having a concentration of about 1 M.

The oxidizing agent in the mixture can be any suitable oxidizing agent. In an embodiment, the oxidizing agent is ozone, nitric acid (HNO₃), hydrogen peroxide (H₂O₂), O₂, bubbled air, I₂, Br₂, Cl₂, oxone™, an ammonium polyatomic salt (e.g., ammonium chlorite, ammonium periodate (NH₄IO₃), ammonium perborate (NH₄BO₃), ammonium chlorate (NH₄ClO₃), ammonium persulfate (NH₄)₂S₂O₈), ammonium hypochlorite or ammonium nitrate), calcium hypochlorite, a sodium polyatomic salt (e.g., sodium persulfate (Na₂S₂O₈), sodium nitrate or sodium hypochlorite), a potassium polyatomic salt (e.g., potassium permanganate, potassium persulfate, potassium iodate, potassium hypochlorite or potassium nitrate), manganese oxide, a tetraalkylammonium salt (e.g., tetramethylammonium chlorite (N(NH₃)₄)ClO₂) or tetramethylammonium periodate (N(NH₃)₄)IO₄)), peroxomonosulfuric acid, urea, peracetic acid, an alkanesulfonic acid (e.g., methane sulfonic acid), an aromatic sulfonic acid (e.g., benzenesulfonic acid) or combinations thereof. In another embodiment, the oxidizing agent is selected from H₂O₂, Cl₂, Br₂, I₂, Ca(ClO)₂, HNO₃, MnO₂, KMnO₄ and K₂Cr₂O₇. In another embodiment, the oxidizing agent is H₂O₂ or Ca(ClO)₂. In a further embodiment, the oxidizing agent is H₂O₂. It is an embodiment that the oxidizing agent is Ca(ClO)₂. The concentration of the oxidizing agent can be any suitable concentration. For example, water may decrease the leaching efficiency in the methods of leaching gold from a gold-containing substance of the present application. In another embodiment, the oxidizing agent is an aqueous solution of H₂O₂ having a concentration of from about 0.01 M to about 1.0 M. In a further embodiment, the oxidizing agent is an aqueous solution of H₂O₂ having a concentration of from about 0.05 M to about 0.5 M. It is an embodiment that the oxidizing agent is an aqueous solution of H₂O₂ having a concentration of from about 0.1 M to about 0.3 M. In another embodiment, the oxidizing agent is an aqueous solution of CaClO₂ having a concentration of from about 0.005 M to about 0.5 M. In a further embodiment, the oxidizing agent is an aqueous solution of CaClO₂ having a concentration of from about 0.01 M to about 0.2 M. It is an embodiment that the oxidizing agent is an aqueous solution of CaClO₂ having a concentration of from about 0.03 M to about 0.1 M.

The water-miscible or partially water-miscible organic solvent can be any suitable water-miscible or partially water-miscible organic solvent including organic acids such as acetic acid. In an embodiment, the water-miscible or partially water-miscible organic solvent in the mixture is selected from acetic acid, ethyl acetate, acetonitrile, tetrahydrofuran (THF), dimethylformamide (DMF), dimethyl sulfoxide (DMSO) and methanol (MeOH). In another embodiment, the water-miscible or partially water-miscible organic solvent is selected from acetic acid, ethyl acetate, acetonitrile and THF. In a further embodiment, the water-miscible or partially water-miscible organic solvent is selected from acetic acid, ethyl acetate and acetonitrile. In another embodiment, the water-miscible or partially water-miscible organic solvent is ethyl acetate or acetonitrile. It is an embodiment that the water-miscible or partially water-miscible organic solvent comprises, consists essentially of or consists of ethyl acetate. In another embodiment, the water-miscible or partially water-miscible organic solvent comprises, consists essentially of or consists of acetonitrile. In a further embodiment, the water-miscible or partially water-miscible organic solvent comprises, consists essentially of or consists of acetic acid.

In an embodiment, the mixture further comprises a metal halide, an ammonium halide or a tetraalkylammonium halide, or a combination thereof. In an embodiment, mixture comprises a metal halide and the metal halide is an alkali metal halide, an alkaline earth metal halide or an aluminium halide, or a combination thereof. In an embodiment, the metal halide is sodium halide, potassium halide, lithium halide, calcium halide, magnesium halide or aluminum halide, or a combination thereof. In an embodiment, the tetraalkylammonium halide is a tetra(C₁₋₄alkyl)ammonium halide, such as tetramethylammonium chloride. In an embodiment, the ammonium halide is ammonium bromide or ammonium chloride, or a combination thereof. In another embodiment of the present application, the mixture further comprises a reagent selected from NaCl, KCl, NaBr, KBr, NaI, KI, CaCl₂, MgCl₂, NH₄Br, NH₄Cl and N(CH₃)₄Cl, or a combination thereof. In a further embodiment, the mixture further comprises the metal halide and the metal halide is CaCl₂, It is an embodiment that the CaCl₂ in the mixture has a concentration of about 0.05M to about 1.5M, about 0.3M to about 0.8M or about 0.6M. In another embodiment, reagent (a) in the mixture is HCl, reagent (b) in the mixture is H₂O₂ and reagent (c) in the mixture is acetic acid.

The substance comprising gold, palladium and/or platinum can be any suitable substance comprising gold, palladium and/or platinum. In an embodiment, the substance comprising gold, palladium and/or platinum is selected from a gold-containing ore, anode slime, a platinum group metal (PGM)-containing substance such as a PGM concentrate, electronic scrap and jewelry scrap.

In an embodiment, the substance comprising gold and/or palladium is a gold-containing substance. In another embodiment of the present application, the gold-containing substance is a gold-containing ore. In another embodiment of the present application, the gold ore is an oxidized gold ore. In another embodiment, the gold ore is a refractory gold ore.

In an embodiment, the gold-containing substance further comprises iron, copper, cobalt, or nickel or a combination thereof, and the method selectively dissolves the gold from the gold-containing substance.

In an embodiment, the method provides a gold dissolution rate of at least 500 gm⁻² h⁻¹, at least 1000 gm⁻² h⁻¹ or at least 5000 gm⁻² h⁻¹. In another embodiment, the method provides a gold dissolution rate of about 500 gm⁻² h⁻¹ to about 9500 gm⁻² h⁻¹ or about 1000 gm⁻² h⁻¹ to about 9500 gm⁻² h⁻¹.

In an embodiment, the substance comprising gold, palladium and/or platinum is a palladium-containing substance. In another embodiment of the present application, the palladium-containing substance is a palladium-containing ore. In an embodiment, the substance comprising gold, palladium and/or platinum is a platinum-containing substance. In another embodiment of the present application, the platinum-containing substance is a platinum-containing ore.

In an embodiment, the substance comprising gold, palladium and/or platinum is a platinum group metal-containing substance. In another embodiment, the platinum group metal-containing substance is a platinum group metal concentrate. It will be appreciated by a person skilled in the art that after dissolution of substances containing platinum group metals including platinum, palladium, rhodium, osmium, ruthenium and iridium the compounds of Formula I can selectively extract both palladium and gold into the organic phase and separate them from the rest of the platinum group metals.⁴⁹

In another embodiment of the present application, the method comprises crushing and/or grinding the substance comprising gold, palladium and/or platinum such as the gold-containing ore into particles prior to contacting with the mixture. In a further embodiment, the size of the particles of the substance comprising gold, palladium and/or platinum such as the gold-containing ore is less than or equal to about 75 microns.

The following non-limiting examples are illustrative of the present application:

EXAMPLES Example 1 New Leaching Methods Employing Sulfur-Based Ligands for Selective Extraction and Recovery of Gold General Ligand Syntheses

The ligands I(a)(i), I(a)(ii), I(a)(iii) and I(a)(iv) (Scheme 2) used in this research were synthesized by following reported literature procedures.⁴⁹ The ligand I(b)(i) (N-phenyl-N′-benzoylthiourea) was synthesized based on a reported procedure.⁵⁰

For example, for ligands I(a)(i)-I(a)(iv), in a round bottom flask, 1.1 equivalents of a substituted amine was added in small portions over a period of 1 hour to a mixture of 1.3 equivalents of CS₂ and 1 equivalent of carbodiimide in methanol at room temperature. The reaction mixture was stirred for 4 hours, and then the resulting white precipitate was separated from the solution by filtration. Finally, it was washed with water and dried under vacuum.

Ligand L₁ Synthesis

In a round bottom flask, 2.02 g pyrrolidine was added in small portions over a period of 1 hour to a mixture of 2.80 g CS₂ and 5.85 g of dicyclohexylcarbodiimide (DCC) in 30 ml methanol at room temperature. The reaction mixture was stirred for four hours, and then the resulting white precipitate was separated from the solution by filtration. Finally, it was washed with water and dried under vacuum. 8.93 g final product was isolated (yield: 89%).

Preparation of Gold Powder

Gold powder was prepared by adapting the reported method from Jeffrey et al.⁵¹. 1.000 g pure (99.9% purity) metallic gold was dissolved in 4 mL aqua regia (3 mL 37% HCl/1 mL 69% HNO₃) and then diluted 5 times by adding distilled water. Sodium metabisulfite was gradually added to the solution while it was being stirred gently. Addition of Na₂S₂O₅ was continued until all of the gold was precipitated out from the solution (the color changed from a yellow to a colorless solution). The resulting precipitate was isolated, washed with 1M HCl and then with distilled water and finally dried in an oven. 0.975 g light brown gold powder was obtained (yield: 97.5%).

(a) Simultaneous Leaching and Solvent Extraction Effect of HCl Concentration

5.0 mg gold powder (0.025 mmol) was added to a vial containing 5 ml HCl solution with different concentrations (0.1, 0.5, 1, 1.5 and 2M) and 0.22 M HNO₃. Then, 26.8 mg (0.075 mmol) ligand I(a)(i) was dissolved in 5 ml dichloromethane and added to the previous solution. The reaction mixture was stirred vigorously for different periods of time. When the reaction was completed, the two phases were separated and the organic phase was stripped with 5 ml 1M H₂SO₄ 1 M containing 0.7 M thiourea for 15 min.

The gold content of the strip solutions was analyzed by AAS. Initial investigations (Table 1) showed that there was a significant difference between conventional leaching by HCl/HNO₃ versus simultaneous leaching and extraction employing dithiobiuret ligands (entry 3 vs 4). While not wishing to be limited by theory, the initial tiny amount of leached gold is extracted into the organic phase by the sulfur-based ligands, pushing forward the gold leaching equilibrium (Scheme 1) which leads to increased leaching kinetics.

The results showed no significant gold recovery at low HCl concentration (entry 1, 2). However, by increasing HCl concentration gold could be completely recovered at 1M HCl or higher. As can be seen in table 1, more than 99% recovery was achieved in 4 hours when HCl concentration was 1M (entry 4), and at higher molarity the recovery time was shorter (entry 5, 6). Therefore, 1 M (mol/L) HCl was chosen as an acid concentration for other experiments.

Effect of Stirring Time

5.0 mg gold powder (0.025 mmol) was added to a vial containing 5 ml 1M HCl and 0.22 M HNO₃. Then, 26.8 mg (0.075 mmol) ligand L₁ was dissolved in 5 ml dichloromethane and added to the previous solution. The reaction mixture was stirred vigorously for different periods of time. When the reaction was completed, the two phases were separated and the organic phase was stripped with 5 ml H₂SO₄ (1M) containing 0.7 M thiourea for 15 min. The gold content of the strip solutions was analyzed by AAS. The results obtained (FIG. 2) showed that the gold recovery percentage increased quickly with the simultaneous leaching and extraction system until it reached 99% after 4 hours and remained constant. This is significantly quicker than conventional leaching systems with the same amount of HCl and HNO₃. A useful leaching time for Au recovery using the present system was found to be 4 h in 1M HCl solution.

A comparison of the conventional leaching system to that of the present study shows that the dithiobiuret ligands can efficiently improve the rate of gold leaching with the least amount of acid and oxidizing reagent. In addition to the leaching step, the new technique recovers gold from aqueous solution at the same time; hence the overall time of gold recovery can be much shorter in comparison to cyanide leaching followed by activated carbon adsorption.

Effect of Ligand Concentration

5.0 mg gold powder (0.025 mmol) was added to a vial containing 5 ml 1M HCl and 0.22M HNO₃. Then, different amounts of ligand L₁ (Table 2) were dissolved in 5 ml dichloromethane and added to the previous solution. The reaction mixture was stirred vigorously for 4 h. When the reaction was completed, the two phases were separated and the organic phase was stripped with 5 ml H₂SO₄ (1M) containing 0.7 M thiourea for 15 min. The gold content of the strip solutions was analyzed by AAS.

Table 2 shows the gold recovery percentage with different ligand to Au ratios. With a 1:1 molar ratio, only 42% of gold was recovered with optimized HCl and oxidant concentrations. Gold recovery increased with increasing ligand concentration in organic solvent and substantially completed at a 3:1 molar ratio (L:Au).

Efficiency of Different Ligand Derivatives

Different derivatives of dithiobiuret ligand (I(a)(i) to I(a)(iv)) were synthesized and their capabilities were investigated for simultaneous leaching and extraction of gold in HCl media (Scheme 2). Compared to a monodentate thiourea derivative (L₁) and conventional gold extractant, dibutylcarbitol (DBC), all of the dithiobiuret derivatives showed a higher percent gold recovery.

Among the different dithiobiuret derivatives (I(a)(i) to I(a)(iv)), I(a)(i) showed the highest Au recovery %. DBC is the most common gold extractant which is used for selective extraction of gold from acidic solution. Although it is an effective gold extractant in conventional solvent extraction techniques, it showed very low gold recovery under the present simultaneous leaching and extraction conditions even at extremely high concentrations of extractant (entry 6, Table 3).

The ligand l(b)(i) was also investigated. 5.0 mg gold powder (0.025 mmol) was added to a vial containing 5 ml HCl (1M) and HNO₃ (0.22 M). Then, 20.3 mg (0.075 mmol) of the synthesized ligand I(b)(i) was dissolved in 5 ml dichloromethane and added to the previous solution. The reaction mixture was stirred vigorously for 6 hours. When the reaction was completed, the two phases were separated and the organic phase was stripped with 5 ml H₂SO₄ (1M) containing 0.7 M thiourea for 15 minutes. The gold content of the strip solutions was analyzed by AAS. The results showed that 99.0% of gold was recovered.

Selectivity

To investigate the selectivity of the present technique, a mixture of different metals in chloride form was treated by the system. A mixture of Fe (1000 ppm), Cu (2000 ppm), Zn (500 ppm), Ag (200 ppm) and 0.5 mg gold powder was added to a vial containing 1M 5 ml HCl and 0.2M HNO₃. Then, 26.8 mg of ligand L₁ was dissolved in 5 ml dichloromethane and added to the previous solution. The reaction mixture was stirred vigorously for different periods of time. When the reaction was completed, the two phases were separated and the organic phase was stripped with 5 ml 1M H₂SO₄ containing 0.7 M thiourea for 15 min. The metal content of the post extraction and strip solutions were analyzed by AAS.

The obtained results, shown in Table 4, demonstrate that the simultaneous leaching and extraction technique employing dithibiuret ligands is highly selective for gold, so that only trace amounts of base metals is extracted even at the presence of high amount of free ligand. In contrast to the cyanidation process, the present technique can, for example eliminate the entire activated carbon step for separation of gold from other impurities.

Effect of Organic Solvent

Simultaneous leaching and extraction tests were performed in the water-immiscible organic solvents shown in Table 5. The results show many organic solvents are suitable for extraction and recovery of gold. Among the investigated solvents, the highest percentages of Au recovery were obtained when dichloromethane (DCM), chlorobenzene, or chloroform were used as solvent.

(b) Gold Ore Treatment

Crushed and ground gold ore with an average gold concentration of 7 ppm and an average particle size of 74 microns was obtained from Claude Resources from their Seabee gold mine operation located in the La Ronge Mining District at the north end of Laonil Lake approximately 125 kilometres northeast of the town of La Ronge, Saskatchewan.

General Experimental for Simultaneous Leaching and Solvent Extraction:

A method flow chart for the simultaneous leaching and solvent extraction technique 200 of the present example is shown in FIG. 3. In the method 200, crushed and ground gold ore 202 with an average particle size of 74 microns was subjected to a simultaneous leaching and extracting step 204 wherein the ore 202 was added to a 1M HCl solution in the presence of HNO₃; and a solution of ligand I(a)(i) in dichloromethane was then added to the aqueous solution 206. The resulting biphasic reaction mixture was stirred vigorously for 5 h. The mixture was then filtered to remove solid residue 208 and the phases separated 210 into an organic phase 212 and an aqueous phase 214. The aqueous phase 214 can be recycled for use in the simultaneous leaching and extracting step 204. The organic phase 212 was then stripped 216 with 1M H₂SO₄ containing 0.7 M thiourea 218 for 15 min, and the gold content of the stripped solutions was analyzed by AAS showing gold recovery efficiencies consistently in the 95-97% range. Subsequent to the stripping step 216, the ligand and DCM can be recycled 220 for use in the simultaneous leaching and extraction step 204. An electrowinning or reduction step 222 can be carried out to isolate pure gold 224. Alternatively, instead of stripping step 216, the organic phase 212 can be reduced with an agent such as oxalic acid or NaBH₄ 226 to provide pure gold 228. If the organic phase is sensitive to a reducing agent, the use of thiourea stripping 216 of gold from the dithiobiuret gold complex may be used. However, the direct reduction 226 of the loaded organic phase may be more economical. For example, in methods 200 comprising stripping 216 the organic phase, a subsequent electrowinning or reduction step 222 is used to obtain the metallic gold 224 whereas in methods 200 comprising a direct reduction step 226, the metallic gold 228 can be obtained with one less step. In the present experiments, because low concentrations of gold in the samples were used, and the efficiency of the systems was measured, the final gold solutions were analyzed. Instead of weighing the precipitated gold, therefore the organic phase was typically stripped and its gold content measured by AAS.

Exemplary Experimental for Simultaneous Leaching and Solvent Extraction:

5.0 g of crushed and ground gold ore with an average particle size of 74 microns was added to a vial containing 5 ml of 1M HCl and 0.55 M HNO₃. 27.8 mg of ligand I(a)(i) dissolved in 5 ml of dichloromethane was then added to the aqueous solution. The reaction mixture was stirred vigorously for 5 h. The biphasic reaction mixture was then filtered and the organic phase was isolated. The organic phase was then stripped with 5 ml H₂SO₄ (1M) containing 0.7 M thiourea for 15 min, and the gold content of the stripped solutions was analyzed by AAS. The final solution contained 6.7 ppm gold (96% gold recovery).

(c) Comparative Example: Gold Ore Treatment with Cyanide Solution:

5.00 g gold ore was added to a vial containing 10 ml basic solution (pH=10.5, pH was adjusted by dissolving the appropriate amount of KOH in distilled water). 0.20 g KCN was added to the solution and the reaction mixture (open to air) was stirred vigorously for 24 hours. The reaction mixture was weighed before starting and after completion of the reaction to estimate the amount of water evaporated during the leaching process. Then the appropriate amount of water was added to the reaction mixture to keep the slurry's density constant. The gold content of the resultant solution was measured by atomic absorption spectroscopy.

This experiment was conducted to determine the amount of gold in the ore sample and to compare the efficiency of the solvent extraction technique of the present studies with the cyanide leaching process. The cyanidation experiment was repeated 20 times on gold ore from the Claude Resources mine, and the results showed the average gold content was between 9.5 and 10 ppm.

(d) Discussion: Solvent Extraction Technique as a Leaching Technique

Appropriate sulfur-containing compounds are useful candidates for gold recovery from ores, because in conformity with Pearson's concept of “hard acid/soft acid and hard base/soft base”, precious metals such as gold are typically classified as soft acids while sulfur containing compounds are classified as soft bases. Therefore, appropriate sulfur containing ligands, such as chelating ligands, can be used as highly selective extractants for extraction and recovery of gold⁴⁹.

Compounds of Formula I wherein, for example, R¹ is —NR⁴R⁵; X is S; and Y and R²-R⁵ are as defined herein are useful for selective extraction of precious metals such as gold from aqueous solutions. Compounds of Formula I wherein, for example, R¹ is aryl; X is O; and R¹-R³ are as defined herein are also useful for selective extraction of precious metals such as gold from aqueous solution. For example, when X is S, the ligand has two strong donor sites (thiocarbonyl groups) to bind with precious metals which make it a strong bidentate ligand which can form highly stable six-membered ring complexes with precious metals like gold (e.g. compounds of Formula II(a) wherein M comprises a precious metal e.g. Au; and Y and R²-R⁵ are as defined herein).

In addition, based on the resonance contributors depicted in Scheme 3, the nitrogen atoms will increase the Lewis basicity at the sulfur atoms, making the sulfur electrons more available to donate to the metal center (further resonance contributors exist when Y═N or S rather than C).

Ligands wherein X═O and R¹=aryl behave similarly but were found to take longer to dissolve the gold; e.g. six hours to completely dissolve gold compared to four hours for the dithiobiuret ligands (X═S) studied.

In a typical known solvent extraction process, the desired metal would first be dissolved into water using large amounts of acid in the presence of an oxidant such as hydrogen peroxide or HNO₃. In a second step, the metal would then be extracted into an organic phase. Subsequent processing would then usually be required to remove other metal impurities that were also extracted in the process. The solvents would then be removed and the desired metal would be reduced back to its base metal form.

Hydrochloric acid in combination with strong oxidants like HNO₃, H₂O₂ and Cl₂ is a well-known leaching media for gold and other transition metals, but high efficiency is only achieved when high concentrations of acid and oxidant are used. By decreasing the hydrochloric acid concentration in known processes, the leaching kinetic decreases dramatically. However, by keeping the oxidant and HCl concentrations high, their consumption will not be economical and produces a highly corrosive media. In addition, in the case of gold ores, the temperature also is typically increased to obtain an effective leaching.

The derivative of dithiobiuret shown in Scheme 4 has been disclosed as a ligand for selective extraction of gold from hydrochloric acid media⁴⁹.

In the present studies, both leaching and extraction steps are done simultaneously under mild conditions which increased the overall efficiencies of the process. As shown in Scheme 1, above, this is accomplished by forcing the reaction equilibrium to the right by withdrawing the dissolved gold from aqueous solution containing small amounts of acid and oxidant into the organic phase containing the ligand. In such a process, highly efficient ligands are used which are able to extract even very small amounts of dissolved gold.

In known processes, solvent extraction is usually applied after the leaching step. As far as the inventors are aware, performing both steps at the same time to improve the leaching step (as well as overall extraction rates) has never been reported before.

Example 2 Simultaneous Leaching and Solvent Extraction of Palladium

5.0 mg palladium powder (0.047 mmol) was added to a vial containing 5 ml water containing HCl (1M) and HNO₃ (0.22 M). Then, 64.95 mg (0.184 mmol) of ligand I(a)(i) was dissolved in 5 ml dichloromethane and added to the previous solution. After 2 hours, the palladium was completely dissolved. The two phases were separated and the organic phase (dark brown) was stripped with 5 ml H₂SO₄ (1M) containing 0.7 M thiourea for 15 minutes. Then, the yellow precipitate was filtered off and heated up in a furnace to 700° C. to produce a fine black palladium powder (99.3% of palladium was recovered).

Example 3 Gold Leaching in Organic Solvents

A mixture of hydrochloric acid and hydrogen peroxide was chosen as leaching reagent in different water-miscible or partially water-miscible organic solvents. 5.0 mg gold powder was added to 5 ml organic solvent containing 500 mg concentrated HCl (37% w/w) and 60 mg H₂O₂ (30% w/w) and stirred for different time periods. After the reaction was complete, the dissolved gold was precipitated and the resultant precipitate was dissolved in aqua regia and purified by the solvent extraction system.⁴⁹ The gold content of the final solution was analyzed by AAS. In the case of incomplete gold dissolution, the loaded organic phase was separated from the leftover gold by filtration.

Among the different solvents shown in Table 6, both ethyl acetate and acetonitrile showed the highest % Au leaching in a very short time (14 min), in spite of low concentrations of HCl (1M) and oxidant (0.1 M). These results showed a very short leaching time by ethyl acetate or acetonitrile solutions containing small amounts of both HCl and H₂O₂.

Table 7 provides an overview of the results of gold leaching in ethyl acetate, acetic acid and acetonitrile containing different concentrations of HCl and oxidant (H₂O₂ or Ca(ClO)₂)) in comparison to a system using aqua regia. In each of the trials, 5.0 mg gold powder was dissolved in 5 mL of the organic solvent which contained different amounts of HCl and oxidant as specified in Table 7. Much higher concentrations of oxidant (HNO₃) and HCl are used for the aqua regia system than for the systems using the organic solvents.

The leaching rates observed in these experiments are fast enough that particle size is not so much of an issue.

General Experimental Details for Gold Ore Leaching in Ethyl Acetate, Acetic Acid, or Acetonitrile:

A method flow chart for a method 300 comprising leaching in a water-miscible or partially water-miscible organic solvent such as ethyl acetate, acetic acid or acetonitrile is shown in FIG. 4. This technology is useful for high efficiency gold leaching using, for example, low concentrations of HCl and H₂O₂ in ethyl acetate, acetic acid or acetonitrile instead of water. In the method 300, crushed and ground gold ore 302 was subjected to leaching step 304 by being added to a water-miscible or partially water-miscible organic solvent such as ethyl acetate, acetic acid or acetonitrile with a 1M concentration of HCl and 0.1 M H₂O₂ 306. The resulting mixture was stirred for 4 h. The ethyl acetate or acetonitrile was separated from the solid residue 312 to obtain a solution of dissolved gold (HAuCl₄) in ethyl acetate, acetic acid or CH₃CN 310 which was then evaporated 314 under vacuum. The resulting precipitate was then dissolved in 0.1 M HCl and the gold was extracted by a solvent extraction process 316 employing I(a)(i) in DCM and finally stripped (not shown) with H₂SO₄ (1 M) containing 0.7 M thiourea.⁴⁹ The resulting gold contents were determined by AAS demonstrating, for example, a minimum of 99% gold recovery efficiencies. After being stripped, the organic phase can be reduced 318 to obtain pure gold 320. In an alternative pathway, the solution of dissolved gold (HAuCl₄) in ethyl acetate, acetic acid or CH₃CN 310 is reduced with an agent such as NaBH₄, ferrocene, Fe powder or Zn powder 322. Using a process comprising such a reduction step 322 instead of the above-described process comprising evaporation step 314 may provide certain advantages, for example, because evaporating the solvent is an additional expense requiring, for example energy and elevated temperatures to evaporate the solvent. By reducing the gold with one of the aforementioned reducing agents, the evaporating step 314 can be eliminated and the solvent can be directly recycled. The gold thereby obtained after the reduction step 322 can then be subjected to a solvent extraction process 324 employing, for example, I(a)(i) in DCM and stripped (not shown) with 1M H₂SO₄ containing 0.7 M thiourea. After being stripped, the organic phase is reduced 326 to obtain pure gold 328. The ethyl acetate, acetic acid or CH₃CN which was removed after the reduction step 322 can be recycled 330 for use in the leaching step 304. The solvent extraction steps (316, 324) in the method 300 are useful, for example, to remove impurities such as copper which can be reduced along with gold. Such solvent extraction steps (316, 324) may comprise a conventional leaching and solvent extraction step (i.e. leaching in aqua regia) or alternatively, may comprise, for example, a method of leaching and extracting gold from a gold-containing substance in one step as described herein.

Exemplary Experimental Details for Gold Ore Leaching in Ethyl Acetate, Acetic Acid or Acetonitrile:

5.0 g of crushed and ground gold ore with an average particle size of 74 microns was added to 5 ml ethyl acetate, acetic acid or acetonitrile containing 350 mg concentrated HCl and 200 mg H₂O₂ 30% w/w. The resulting mixture was stirred for 4 h. The ethyl acetate, acetic acid or acetonitrile was separated from the solid residue and evaporated under vacuum. The resulting precipitate was then dissolved in 2 ml 0.1M HCl and the gold was extracted by a solvent extraction process employing 27.2 mg I(a)(i) in 2 ml DCM and finally stripped with 2 ml 1M H₂SO₄ containing 0.7 M thiourea. The resulting gold contents were determined by AAS demonstrating 96-97% gold recovery efficiencies.

Example 4 Reduction of Leached Gold in Different Organic Solvents

For each test, 5 ml of organic solvent (which contained 0.5 grams of 37% HCl; i.e. the molarity of the HCl in the organic solvent was 1M) containing different amounts of gold as shown in Table 8 was treated with the indicated reducing reagent for 10 minutes. In the case of Fe powder, the stirring time was 2 hours. The concentration of gold solutions was measured by AAS.

Example 5 Dissolution of Palladium in Organic Solvents

A mixture of hydrochloric acid and hydrogen peroxide was chosen as leaching reagent in different water-miscible or partially water-miscible organic solvents (ethyl acetate, acetic acid, or acetonitrile). 5.0 mg palladium powder (200 mesh) was added to a stirred mixture of 5 ml organic solvent (ethyl acetate, acetic acid, or acetonitrile) containing 500 mg concentrated HCl (37% w/w) and 60 mg H₂O₂ (30% w/w) at room temperature. After 15 minutes, the palladium powder was completely dissolved and a clear red solution was obtained.

Example 6 Dissolution of Platinum in Organic Solvents

To a stirred organic solvent (ethyl acetate, acetic acid, or acetonitrile) containing 500 mg concentrated HCl (37% w/w) and 60 mg H₂O₂ (30% w/w), 5 mg platinum powder (200 mesh) was added at room temperature. After 90 minutes, the platinum powder was completely dissolved and a pale yellow colored solution was obtained.

Example 7 Effect of Halide Salt Addition to Acid Mixtures (a) Measuring the Rate of Gold Dissolution

120 mg (0.610 mmol) of gold wire (99.9%) with a diameter of 0.25 mm was placed in 20 ml acetic acid containing the desired amounts of acid, oxidant and optionally CaCl₂ and stirred at 800 rpm (stir plate setting) for varying time periods (10-60 min) at varying temperatures. The remaining gold wire was then removed from the reaction mixture, washed with acetone and air-dried. The remaining wire was then weighed to calculate the amount of dissolved gold. Based on wire diameter, mass change and dissolution time a dissolution rate was then determined. Table 9 shows the rate of gold dissolution under varying conditions at room temperature. FIG. 5 shows a comparison between the gold dissolution rate of aqua regia, concentrated HCl/H₂O₂ and acetic acid systems. Reagent concentrations in acetic acid were HCl (1.5 M), H₂O₂ (0.6 M), and CaCl₂ (0.6 M). The HCl/H₂O₂ mixture was freshly prepared by mixing 4 parts of conc. HCl with one part of H₂O₂ 30%.

(b) Gold Ore Treatment

5.00 g of gold ore was added to the desired amounts of acetic acid (5.0 ml or 10.0 ml) containing the desired amounts of HCl, H₂O₂ and CaCl₂. The resulting mixture was stirred at 800 rpm for varying time periods. The acetic acid was separated from the solid residue by centrifuge (1 min) and evaporated under vacuum. The resulting residue was then dissolved in 2.0 ml of 1M HCl and its gold content was determined by ICP-OES (Table 10).

(c) Selective Gold Stripping from Printed Circuit Boards

20 g printed circuit boards (PCBs) without shredding were added to a 100 ml acetic acid solution including 0.5 M HCl, 0.2 M CaCl₂ and 0.2 M H₂O₂, and stirred for 2 min. The treated pieces were separated and washed with water, then treated with hot aqua regia to see if any gold was left. ICP revealed that more than 99% of gold was leached while less than 5% of Ni and 1% of copper were dissolved. The same solution was reused 75 times for leaching gold from new PCBs before any loss in activity was observed (i.e. 1.5 kg PCBs were treated with 100 ml HOAc solution in total).

Gold leaching from PCBs using the HOAc system (including 0.5 M HCl, 0.2 M H₂O₂ and 0.2 M CaCl₂) at r.t in less than 20 seconds resulted in selective gold dissolution (i.e. the underlying nickel was still present).

(d) Results and Discussion

Disclosed herein is a new gold leaching system with the highest gold dissolution rate published to date. This system employs acetic acid as a solvent and contains very low concentrations of an additional acid and an oxidant. Along with an unmatched gold dissolution rate, this new leaching system is also highly selective for gold over base metals such that gold can be dissolved even faster than iron, nickel, cobalt and copper. The efficiency of this new leaching system was examined on gold ore, jewelry scrap and electronic waste (scraps), resulting in >99% of gold leaching at room temperature in only 25 minutes, 10 minutes and 10-20 seconds respectively.

A gold dissolution rate of 6020 gm⁻² h⁻¹ for gold (three times faster than that of aqua regia) at room temperature has been obtained by using acetic acid as solvent under mild conditions (Tables 9, 11). This result represents the fastest recorded rate known for gold dissolution in either organic or aqueous systems (considerably faster than any other known system). Heating the system to 60° C. increases the gold dissolution rate even further to 9000 gm² h⁻¹ (Table 11).

As also can be seen from entries 13 and 14 in Table 11, conducting the dissolution using acetic acid as the solvent resulted in a dramatically higher gold dissolution rate (6020 gm⁻² h⁻¹) in comparison to the gold dissolution rate (5.1 gm⁻² h⁻¹) obtained for a comparative system which used water as the solvent.

In addition to its substantially faster dissolution kinetics, this new leaching method has a much higher affinity for gold over base metals in comparison to concentrated HCl/H₂O₂ and aqua regia systems, resulting in gold being dissolved faster than most base metals (FIG. 6).

This selectivity results in reduced reagent consumption and contributes to making this extraction technique more economical than both aqua regia and concentrated HCl/H₂O₂.

This acetic acid process is not only the fastest gold dissolution system known, it is also, for example, easy to perform, energy efficient and safer than aqua regia or cyanide systems. By being recyclable, the acetic acid system generates the least amount of liquid waste compared to other systems and also eliminates the requirement for massive water consumption compared to the cyanidation process which can lead to widespread applications of this new technology in remote gold mines which do not have access to water sources. Table 11 compares the efficiency of this extraction method based on the rate of gold dissolution with reported leaching systems. The acetic acid process is substantially more efficient than the reported leaching methods while maintaining mild operating conditions. The fast kinetics of the new leaching system along with low reagent consumptions, simple chemistry, ambient temperature processing and use of commercially available and more environmentally benign reagents make this new leaching system of use for large-scale operations of gold extraction from all gold-bearing materials.

While the present application has been described with reference to examples, it is to be understood that the scope of the claims should not be limited by the embodiments set forth in the examples, but should be given the broadest interpretation consistent with the description as a whole.

All publications, patents and patent applications are herein incorporated by reference in their entirety to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety. Where a term in the present application is found to be defined differently in a document incorporated herein by reference, the definition provided herein is to serve as the definition for the term.

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TABLE 1 Simultaneous leaching and extraction of gold powder in different HCl concentrations. HCl Time Au Recovery Entry (M) (h) (%) 1 0.1 4 5.3 2 0.5 4 20.7 3 1 4 4.6* 4 1 4 99.2 5 1.5 3 99.1 6 2 2.5 99.3 *Conventional leaching by HCl/HNO₃.

TABLE 2 Simultaneous leaching and extraction of gold powder with different ligand:Au ratios. Au Recovery Entry Ligand:Au % 1 1:1 42.7 2 2:1 72.4 3 3:1 99.5 4 4:1 99.4

TABLE 3 Simultaneous leaching and extraction of gold powder with different ligands. Au Recovery Entry Ligand % 1 I(a)(i) 99.7 2 I(a)(ii) 72.4 3 I(a)(iii) 96.5 4 I(a)(iv) 70.4 5 L₁ 3.3 6 DBC 5.1* *Pure DBC was used as the organic phase.

TABLE 4 Effect of other impurities on simultaneous leaching and extraction of gold (113 ppm of gold was extracted in the presence of large excesses of Fe, Cu and Zn impurities). Fe Cu Zn Au Aq phase (ppm) 991.8 2140.3 542.8 0.3 Stripping solution (ppm) 0.4 0.1 0.1 112.3

TABLE 5 Simultaneous leaching and extraction of gold powder in different water-immiscible organic solvents. Au Recovery Entry Solvent % 1 DCM 99.9 2 Chloroform 97.4 3 Dichloroethane 68.4 4 Chlorobenzene 98.8 5 Dichlorobenzene 61.3 6 Toluene 56.1

TABLE 6 Gold leaching in different water-miscible organic solvents containing HCl and H₂O₂ Stirring Au Time Leaching Entry Solvent (h) % 1 THF 0.5 24 2 THF 5 100 3 DMF 24 56 4 DMSO 24 31 5 Ethyl acetate 0.25 100 6 MeCN 0.25 100 7 MeOH 24 13

TABLE 7 Gold leaching in different solvents containing different HCl and oxidant concentrations. Stirring Au Oxidant HCl time Leaching Entry Solvent (M) (M) (min) %  1 Ethyl acetate H₂O₂(0.10) 1 14 100  2 Ethyl acetate H₂O₂(0.20) 1 6 100  3 Ethyl acetate H₂O₂(0.30) 1 4 100  4 Ethyl acetate H₂O₂(0.10) 2 4 100  5 Ethyl acetate H₂O₂(0.10) 2 4 100  6 MeCN H₂O₂(0.10) 1 14 100  7 MeCN H₂O₂(0.20) 1 6 100  8 MeCN H₂O₂(0.30) 1 4 100  9 MeCN H₂O₂(0.10) 2 4 100 10 MeCN H₂O₂(0.10) 2 4 100 11 Ethyl acetate Ca(ClO)₂ 1 6 100 (0.03) 12 Ethyl acetate Ca(ClO)₂ 1 4 100 (0.05) 13 Ethyl acetate Ca(ClO)₂ 1 3 100 (0.10) 14 MeCN Ca(ClO)₂ 1 6 100 (0.03) 15 MeCN Ca(ClO)₂ 1 4 100 (0.05) 16 MeCN Ca(ClO)₂ 1 3 100 (0.10) 17 CH₃COOH H₂O₂(0.10) 1 14 100 18 CH₃COOH H₂O₂(0.20) 1 6 100 19 CH₃COOH Ca(ClO)₂ 1 6 100 (0.03) 20 CH₃COOH Ca(ClO)₂ 1 4 100 (0.05) 21 Aqua regia HNO₃ 9.6 8 100 (2.92)

TABLE 8 Reduction of leached gold in different organic solvents. Au Au concentration concentration Reducing before after agent reduction reduction Reduction Entry Solvent (mg) (ppm) (ppm) %  1 Ethyl Zn powder 1000 5 99.5 acetate (20)  2 Ethyl Zn powder 10 0 100 acetate (10)  3 Ethyl NaBH₄ (10) 1000 5 99.5 acetate  4 Ethyl NaBH₄ (5) 10 0 100 acetate  5 Ethyl Fe powder 1000 8 99.2 acetate (20)  6 Ethyl Fe powder 10 0 100 acetate (10)  7 MeCN Zn powder 1000 2 99.8 (20)  8 MeCN Zn powder 10 0 100 (10)  9 MeCN NaBH₄ (10) 1000 6 99.4 10 MeCN NaBH₄ (5) 10 0.3 97.0 11 MeCN Fe powder 1000 12 98.8 (20) 12 MeCN Fe powder 10 0.1 99.0 (10) 13 CH₃COOH Zn powder 1000 1 99.9 (20) 14 CH₃COOH Zn powder 10 0 100 (10) 15 CH₃COOH NaBH₄ (10) 1000 9 99.1 16 CH₃COOH NaBH₄ (5) 10 0 100 17 CH₃COOH Fe powder 1000 8 99.2 (20) 18 CH₃COOH Fe powder 10 0.5 95.0 (10)

TABLE 9 Gold dissolution rate in acetic acid under varying conditions. gold dissolution HCl H₂O₂ CaCl rate Entry (mol/L) (mol/L) (mol/L) (gm⁻² h⁻¹)  1 0.1 0.2 —  350  2 0.2 0.2 —  570  3 0.5 0.2 —  857  4 1.0 0.2 — 1280  5 1.5 0.2 — 1285  6 1.0 0.1 —  850  7 1.0 0.3 — 1310  8 0.5 0.2 0.2 2100  9 1.0 0.2 0.1 1580 10 1.0 0.2 0.2 2110 11 1.0 0.2 0.3 2120 12 1.0 0.3 0.3 2940 13 1.0 0.4 0.4 3700 14 1.0 0.5 0.5 3720 15 1.5 0.4 0.4 4500 16 1.5 0.6 0.6 6020 17 1.5 0.8 0.8 6018 18 2.0 0.8 0.8 5810 19 3.0 1.2 1.2 4100

TABLE 10 Gold ore leaching results by cyanidation process vs acetic acid system under varying conditions at room temperature. Dissolved Sample solvent/solid* Time HCl H₂O₂ CaCl₂ KCN gold # (v/v) (h) (M) (M) (M) (M) (ppm)*** 1 1 10 1 0.4 0.4 — 9.8 2 2 1 1 0.4 0.4 — 10.2 3 2 0.4 1.5 0.6 0.6 — 10.3 4 2 5 0.5 0.2 0.2 — 9.8 5** 2 1.5 0.5 0.2 0.2 — 9.9 6 2 35 — — — 0.02 9.9 *For samples 1-5, the solvent was acetic acid, and for sample 6 it was water with pH = 10.5. **gold leaching was performed at 60 °C. ***Gold concentration in ore was 10.4 ppm.

TABLE 11 Comparison of the rate of gold dissolution in different leaching systems. Solvent Rate Entry Lixiviant solution (t ° C.) (gm⁻² h⁻¹) Ref.  1 glycine, H₂O₂ H₂O (rt)* 0.2 52  2 NaCN, Ca(OH)₂ H₂O (30) 0.7 53  3 Fe³⁺, SC(NH₂)₂, H₂SO₄ H₂O (rt) 7 54  4 SCN⁻, Fe³⁺ H₂O (rt) 7.3 55  5 Cu²⁺, S₂O₃ ²⁻, NH₃ H₂O (rt) 27 54  6 I₂, KI H₂O (35) 36.4 56  7 SOCl₂/py mixture (3:1) SOCl₂ (rt) 59 57  8 OCl⁻, NaCl, pH = 6 HO (rt) 130 58  9 I₂, [NEt₄] I MeCN (80) 189 59 10 CuBr, KBr DMSO (75) 370 60 11 aqua regia conc. HCl/ 1850 present HNO₃ (rt) work 12 conc. HCl/H₂O₂ HCl/H₂O₂ 2320 present (4:1) (rt) work 13 0.6M H₂O₂, 0.6M CaCl₂ H₂O (rt) 5.1 present 1.5M HCl work 14 0.6M H₂O₂, 0.6M CaCl₂ acetic acid 6020 present 1.5M HCl (rt) work 15 0.6M H₂O₂, 0.6M CaCl₂ acetic acid 9000 present 1.5M HCl (60) work *rt = room temperature 

1. A method of leaching palladium and/or platinum from a substance comprising palladium and/or platinum, the method comprising (i) leaching the substance with a first mixture comprising: (a) an acid; (b) an oxidizing agent; and (c) a solvent selected from acetic acid, ethyl acetate, acetonitrile, and tetrahydrofuran to provide a second mixture, the leaching being done under conditions to leach the palladium and/or platinum from the substance, wherein the conditions to leach the palladium and/or platinum from the substance comprise stirring the substance and the first mixture for a time of about 0.1 minute to about 2 hours at a temperature of about 20° C. to about 60° C., the acid is a hydrogen halide, chlorous acid, chloric acid, bromous acid, bromic acid, iodous acid, iodic acid, perchloric acid, sulfuric acid, oxalic acid, phosphoric acid, an organic acid or combinations thereof, and the oxidizing agent is ozone, nitric acid, hydrogen peroxide, O₂, bubbled air, I₂, Br₂, Cl₂, potassium monopersulfate, an ammonium polyatomic salt, calcium hypochlorite, a sodium polyatomic salt, a potassium polyatomic salt, manganese oxide, a tetraalkylammonium salt, peroxomonosulfuric acid, urea, peracetic acid, or combinations thereof; and (ii) separating insoluble impurities from the second mixture to provide a solution of leached palladium and/or platinum.
 2. The method of claim 1, wherein the method further comprises: evaporating the solution to provide the leached palladium and/or platinum.
 3. The method of claim 2, wherein the method further comprises, after evaporating, contacting the leached palladium and/or platinum with a compound of Formula I:

wherein R¹ is —NR⁴R⁵ or aryl; R² and R³ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl; R⁴ and R⁵ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or R⁴ and R⁵ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl; X is O or S; Y is S, NR⁶ or CR⁶R⁷; and R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl, under conditions to form a complex between the compound of Formula I and the leached palladium.
 4. The method of claim 3, wherein Y is NR⁶.
 5. The method of claim 3, wherein the compound of Formula I is a compound of Formula I(a)(i), I(a)(ii), I(a)(iii) or I(a)(iv):


6. The method of claim 3, wherein the conditions to form the complex between the compound of Formula I and the leached palladium comprise contacting the solution with the compound of Formula I in a water-immiscible organic solvent for a time of about 2 minutes to about 30 minutes at a temperature of about 10° C. to about 40° C.
 7. The method of claim 3, wherein the method further comprises stripping the palladium from the complex between the compound of Formula I and the leached palladium by a method comprising contacting the water-immiscible organic solvent containing the complex between the compound of Formula I and the leached palladium with an aqueous solution comprising an acid and thiourea under conditions to obtain a palladium-containing strip solution and a palladium-reduced organic phase comprising the compound of Formula I.
 8. The method of claim 7, wherein the method further comprises separating the palladium-containing strip solution from the palladium-reduced organic phase comprising the compound of Formula I and recovering palladium from the palladium-containing strip solution by electrowinning or reduction.
 9. The method of claim 1, wherein the method further comprises: contacting the solution with a reducing agent under conditions to obtain palladium and/or platinum; and separating the palladium and/or platinum from the solution.
 10. The method of claim 9, wherein the method further comprises, after separating the palladium and/or platinum from the solution: dissolving the palladium and/or platinum in aqua regia; and contacting the dissolved palladium and/or platinum with a compound of Formula I:

wherein R¹ is —NR⁴R⁵ or aryl; R² and R³ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or R² and R³ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl; R⁴ and R⁵ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl; or R⁴ and R⁵ together with the nitrogen atom to which they are attached, form a heterocycloalkyl or a heteroaryl, or a heterocycloalkyl or a heteroaryl substituted at one or more carbon atoms with C₁₋₄alkyl; X is O or S; Y is S, NR⁶ or CR⁶R⁷; and R⁶ and R⁷ are each independently selected from H, C₁₋₁₀alkyl, C₃₋₁₀cycloalkyl, C₁₋₆alkyleneC₃₋₁₀cycloalkyl, heterocycloalkyl and aryl, under conditions to form a complex between the compound of Formula I and the dissolved palladium.
 11. The method of claim 10, wherein the conditions to form the complex between the compound of Formula I and the dissolved palladium comprise contacting the dissolved palladium and/or platinum with the compound of Formula I in a water-immiscible organic solvent for a time of about 2 minutes to about 30 minutes at a temperature of about 10° C. to about 40° C.
 12. The method of claim 11, wherein the method further comprises stripping the palladium from the complex between the compound of Formula I and the dissolved palladium by a method comprising contacting the water-immiscible organic solvent containing the complex between the compound of Formula I and the dissolved palladium with an aqueous solution comprising an acid and thiourea under conditions to obtain a palladium-containing strip solution and a palladium-reduced organic phase comprising the compound of Formula I.
 13. The method of claim 12, wherein the method further comprises separating the palladium-containing strip solution from the palladium-reduced organic phase comprising the compound of Formula I and recovering palladium from the palladium-containing strip solution by electrowinning or reduction.
 14. The method of claim 1, wherein the solvent is selected from acetic acid, ethyl acetate, and acetonitrile.
 15. The method of claim 1, wherein the first mixture further comprises a metal halide, an ammonium halide, a tetraalkylammonium halide or a combination thereof.
 16. The method of claim 1, wherein the substance is a palladium and/or platinum-containing ore, a platinum-group metal concentrate.
 17. The method of claim 1, wherein the solvent is acetic acid.
 18. The method of claim 1, wherein the acid is selected from HCl, H₂SO₄, HBr, H₃PO₄ and HI.
 19. The method of claim 18, wherein the acid is HCl.
 20. The method of claim 19, wherein the acid is present in the first mixture at a concentration of from about 0.01M to about 2.5M.
 21. The method of claim 1, wherein the oxidizing agent is selected from H₂O₂, Cl₂, Br₂, I₂, Ca(ClO)₂, HNO₃, MnO₂, KMnO₄ and K₂Cr₂O₇.
 22. The method of claim 21, wherein the oxidizing agent is H₂O₂ or HNO₃.
 23. The method of claim 22, wherein the oxidizing agent is H₂O₂ and the H₂O₂ is present in the first mixture at a concentration of from about 0.01 M to about 1.0 M.
 24. The method of claim 22, wherein the oxidizing agent is HNO₃ and the HNO₃ is present in the first mixture at a concentration of from about 0.2 M to about 3 M.
 25. The method of claim 1, wherein the conditions to leach the palladium and/or platinum from the substance comprise stirring the substance and the first mixture at a temperature of about 20° C. to about 40° C.
 26. The method of claim 1, wherein step (ii) comprises separating insoluble impurities from the second mixture to provide a solution of dissolved leached palladium and/or platinum that remains in solution at room temperature.
 27. The method of claim 1, wherein the conditions to leach the palladium and/or platinum from the substance comprise stirring the substance and the first mixture at a temperature of about 20° C. to about 25° C.
 28. The method of claim 1, wherein the first mixture comprises less than, or equal to, about 17% (w/w) water.
 29. The method of claim 1, wherein the solvent is a non-aqueous solvent. 